Special

GgaINT1029661 @ galGal4

Intron Retention

Gene
Description
villin-1 [Source:RefSeq peptide;Acc:NP_990773]
Coordinates
chr7:22034258-22034669:-
Coord C1 exon
chr7:22034511-22034669
Coord A exon
chr7:22034438-22034510
Coord C2 exon
chr7:22034258-22034437
Length
73 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGC
5' ss Score
8.7
3' ss Seq
CCTATCCCCGCTGTTCCCAGAAC
3' ss Score
8.19
Exon sequences
Seq C1 exon
GGCCGCCATGCCAGCACGGATGAGCTGGCCGCCTCGGCCTACCAAGCCGTCTTCCTGGACCAGAAGTACAACAACGAGCCTGTGCAGGTGCGCGTCACCATGGGCAAGGAGCCGGCCCACCTGATGGCGATCTTCAAGGGCAAGATGGTGGTGTACGAG
Seq A exon
GTGAGCACGGGGCTGGTGGCAGGGTGGGCAAACTGGTGGCTGTGTGACCTCTTCCTATCCCCGCTGTTCCCAG
Seq C2 exon
AACGGCTCCTCGCGGGCGGGCGGCACGGAGCCGGCGTCCTCCACTCGGCTCTTCCACGTGCACGGCACCAACGAGTACAACACCAAGGCCTTCGAGGTGCCCGTCCGAGCCGCTTCTCTCAACTCCAACGATGTCTTTGTGCTCAAGACGCCCAGCTCCTGCTACCTCTGGTATGGGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011433:ENSGALT00000038192:12
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.067
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PD(49.4=77.4)
A:
NA
C2:
PF0062617=Gelsolin=PU(47.8=55.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TACAACAACGAGCCTGTGCAG
R:
TGGTGTTGTACTCGTTGGTGC
Band lengths:
178-251
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]